chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	207896057	207896058	G	T	34	GENIC	heterozygous	60340299
2	207896119	207896120	A	-	25	GENIC	possibly homozygous	59356681
2	207896125	207896126	T	G	50	GENIC	heterozygous	60340301
2	207896595	207896596	T	C	39	GENIC	homozygous	60340303
2	207896619	207896620	C	T	40	GENIC	homozygous	60340305
2	207897186	207897187	T	C	50	GENIC	homozygous	59356682
2	207898157	207898158	A	AC	13	GENIC	homozygous	59356683
2	207898676	207898677	A	G	41	GENIC	homozygous	59931828
2	207899955	207899956	G	A	36	GENIC	heterozygous	59356684
2	207899959	207899960	G	A	35	GENIC	possibly homozygous	59356685
2	207900001	207900002	A	C	49	GENIC	possibly homozygous	60340307
2	207900005	207900006	A	C	49	GENIC	possibly homozygous	59931831
2	207900009	207900010	A	C	48	GENIC	possibly homozygous	59356687
2	207903157	207903158	T	G	55	GENIC	homozygous	60340309
2	207903595	207903596	G	C	67	GENIC	possibly homozygous	59356688
2	207904314	207904315	A	T	48	GENIC	homozygous	59931833